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Clinical Trials in China / NCT06575257
Recruiting Phase 2

Neoadjuvant Therapy of Darolutamide Plus ADT for High Risk Prostate Cancer

NCT06575257 · tracked via the Priya Life Science China tracker
Phase
Phase 2
Started
2024-05-01
Last updated
2024-08-28

Condition(s) studied

Prostate Cancer

Investigational drug(s) / intervention(s)

Darolutamide →Goserelin 3.6 mg →

Darolutamide: 600 mg orally twice daily for 12 weeks before radical prostatectomy

Goserelin 3.6 mg: 3.6 mg goserelin hypodermic once per 4 weeks

Study summary

The purpose of this study is to determine if treatment with Darolutamide plus androgen deprivation therapy (ADT) before radical prostatectomy (RP) with pelvic lymph node dissection (pLND) in participants with high-risk localized or locally advanced prostate cancer results in an improvement in pathological complete response (pCR) rate and pathological tumor volume with minimal residual disease (MRD)) as compared to ADT.

Eligibility

Sex
MALE
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Patients must be ≥ 18 and ≤75 years of age. * All patients must have a histologically or cytologically diagnosis of prostate cancer and must be eligible for radical prostatectomy. * Eastern Cooperative Oncology Group (ECOG) Performance Status score ≤1. * All patients must complete mpMRI or 68Ga-PSMA PET / CT before and after neoadjuvant treatment. * All patients must undergo thorough tumor staging and meet one of the following criteria: 1. multi-parameter MRI or PSMA PET / CT shows clinical staging of primary tumor ≥ cT2c or cN+or locally advanced, 2. Gleason score of primary tumor ≥ 8, 3. prostate specific antigen (PSA) ≥20 ng/ml. * Patients must have adequate organ function as defined by the following criteria(within 28 days prior to registration): white blood cell (WBC) ≥ 4.0 × 109 / L platelets≥ 100 × 109 / L hemoglobin ≥ 9 g / dL international normalized ratio (INR) \< 1.5. total bilirubin (TBIL)≤1.5 x upper limit of normal (ULN) SGOT (AST) and SGPT (ALT) ≤ 2.5 x ULN serum creatinine ≤2×ULN * Patients must participate voluntarily and sign an informed consent form (ICF), indicating that they understand the purpose and required procedures of the study, and are willing to participate in. Patients must be willing to obey the prohibitions and restrictions specified in the research protocol. Exclusion Criteria: * clinical or radiological evidence of regional or extra-regional lymph node metastases or bone metastases or visceral metastases. * Prior androgen deprivation therapy (medical or surgical) or focal treatment of prostate cancer or prostate cancer radiotherapy or prostate cancer chemotherapy. * severe or uncontrolled concurrent infections. * New York Heart Association Class III or IV congestive heart failure at the time of screening. * uncontrolled severe hypertension, persistent uncontrolled diabetes, oxygen-dependent lung disease, chronic liver disease, or HIV infection. * Patients with mental illness, mental disability or inability to give informed consent are not eligible. * Patients have had other malignancies other than prostate cancer in the past 5 years, but cured basal cell or squamous cell skin cancers can be enrolled.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The First Affillated Hospital, the Air Force Medical University Xi’an Shanxi Recruiting

More Xijing Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06575257 on ClinicalTrials.gov ↗ ← All trials in China